Experience & JOB RESponsibilities
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RESEARCH JOB POSITION 1
2014-Present I Company Name
- Identified, oversaw and collaborated with various vendors that delivered site management and monitoring, central image reading, recruitment and public relations for phase III trial to ensure compliance to protocol and GCP guidelines.
- Compiled and communicated various study metric and summary reports to senior management and company board of directors.
- Key contributor or developer of all study documents including protocol, ICD template, CRFs and data collection tools, CRO oversight plan, site training materials.
- Oversaw site management and monitoring vendor to complete feasibility and selection and start-up of over 90 study sites for US based phase III trial.
- Developed study level recruitment materials and reviewed all site specific materials to align with trial and company messaging.
RESEARCH JOB POSITION 2
2012- 2014 I Company Name
- Identified, oversaw and collaborated with various vendors that delivered site management and monitoring, central image reading, recruitment and public relations for phase III trial to ensure compliance to protocol and GCP guidelines.
- Compiled and communicated various study metric and summary reports to senior management and company board of directors.
- Key contributor or developer of all study documents including protocol, ICD template, CRFs and data collection tools, CRO oversight plan, site training materials.
- Oversaw site management and monitoring vendor to complete feasibility and selection and start-up of over 90 study sites for US based phase III trial.
- Developed study level recruitment materials and reviewed all site specific materials to align with trial and company messaging.
RESEARCH JOB POSITION 3
2010- 2012 I Company Name
- Identified, oversaw and collaborated with various vendors that delivered site management and monitoring, central image reading, recruitment and public relations for phase III trial to ensure compliance to protocol and GCP guidelines.
- Compiled and communicated various study metric and summary reports to senior management and company board of directors.
- Key contributor or developer of all study documents including protocol, ICD template, CRFs and data collection tools, CRO oversight plan, site training materials.
- Oversaw site management and monitoring vendor to complete feasibility and selection and start-up of over 90 study sites for US based phase III trial.
- Developed study level recruitment materials and reviewed all site specific materials to align with trial and company messaging.